Wei Zhong-Ya, Qu Hui-Lin, Dai Yu-Juan, Wang Qian, Ling Zhuo-Min, Su Wen-Feng, Zhao Ya-Yu, Shen Wei-Xing, Chen Gang
Key Laboratory of Neuroregeneration of Jiangsu and Ministry of Education, Co-innovation Center of Neuroregeneration, Nantong University, Nantong, Jiangsu Province, China.
Medical School of Nantong University, Nantong, Jiangsu Province, China.
Neural Regen Res. 2021 May;16(5):899-904. doi: 10.4103/1673-5374.290911.
Pannexin 1 (Panx 1), as a large-pore membrane channel, is highly permeable to ATP and other signaling molecules. Previous studies have demonstrated the expression of Panx 1 in the nervous system, including astrocytes, microglia, and neurons. However, the distribution and function of Panx 1 in the peripheral nervous system are not clear. Blocking the function of Panx 1 pharmacologically (carbenoxolone and probenecid) or with small interfering RNA targeting pannexins can greatly reduce hypotonicity-induced ATP release. Treatment of Schwann cells with a Ras homolog family member (Rho) GTPase inhibitor and small interfering RNA targeting Rho or cytoskeleton disrupting agents, such as nocodazole or cytochalasin D, revealed that hypotonicity-induced ATP release depended on intracellular RhoA and the cytoskeleton. These findings suggest that Panx 1 participates in ATP release in Schwann cells by regulating RhoA and the cytoskeleton arrangement. This study was approved by the Animal Ethics Committee of Nantong University, China (No. S20180806-002) on August 5, 2018.
泛连接蛋白1(Panx 1)作为一种大孔膜通道,对ATP和其他信号分子具有高度通透性。先前的研究已证明Panx 1在包括星形胶质细胞、小胶质细胞和神经元在内的神经系统中表达。然而,Panx 1在周围神经系统中的分布和功能尚不清楚。药理学上使用(甘珀酸和丙磺舒)或用靶向泛连接蛋白的小干扰RNA阻断Panx 1的功能,可大大减少低渗诱导的ATP释放。用Ras同源家族成员(Rho)GTP酶抑制剂、靶向Rho的小干扰RNA或细胞骨架破坏剂(如诺考达唑或细胞松弛素D)处理雪旺细胞,结果显示低渗诱导的ATP释放依赖于细胞内的RhoA和细胞骨架。这些发现表明,Panx 1通过调节RhoA和细胞骨架排列参与雪旺细胞中ATP的释放。本研究于2018年8月5日获得中国南通大学动物伦理委员会批准(编号:S20180806 - 002)。